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Abuta grandifolia

Abuta grandifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440064c102b5801996716
Scientific name Abuta grandifolia
Authority (Mart.) Sandwith
First published in Bull. Misc. Inform. Kew 1937: 37 (1937)

Description Top

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Synonyms Top

Scientific name Authority First published in
Abuta concolor Poepp. & Endl. Nov. Gen. Sp. Pl. 2: 64 (1838)
Abuta concolor Benth. J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 49. 1861
Abuta guianensis Eichl. Flora 47: 390 (1864)
Anelasma concolor Miers Ann. Mag. Nat. Hist. , ser. 3, 14: 260 (1864)
Anelasma gardnerianum Miers Ann. Mag. Nat. Hist. , ser. 2, 7: 43 (1851)
Anelasma guianense Miers Ann. Mag. Nat. Hist. , ser. 2, 7: 43 (1851)
Anelasma laurifolium Sagot ex Benth. J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 50 (1861)
Anelasma laurifolium Miers Ann. Mag. Nat. Hist. , ser. 3, 14: 260 (1864)
Anelasma laurifolium Sagot ex Diels Pflanzenr. IV, 94: 197 1910
Anelasma martianum Miers Ann. Mag. Nat. Hist. , ser. 3, 14: 260 (1864)
Anelasma pallidum Miers Ann. Mag. Nat. Hist. , ser. 3, 14: 260 (1864)
Anelasma spruceanum Miers ex Benth. Hooker's J. Bot. Kew Gard. Misc. 3: 116 (1851)
Cocculus grandifolius Mart. Repert. Pharm. 36: 345 (1830)
Cocculus laevigatus Mart. Flora 24(2 Beibl.): 45 (1841)
Trichoa concolor Endl. ex Walp. Repert. Bot. Syst. 1: 95 (1842)
Trichoa guyanensis Klotzsch ex Eichler Fl. Bras. 13(1): 181 (1864)
Anelasma spruceanum Miers Ann. Mag. Nat. Hist., ser. 3 14: 261 1864

Common names Top

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Language Common/alternative name
Arabic عنيبية سهمية الأوراق
Quechua yawati kaspi
Quechua yawati p'anqa
Quechua yawati panka
Quechua yawati panqa
Quechua yawatik'aspi
Quechua yawatikaspi
Quechua yawatipanka
Quechua yawati k'aspi

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000511646
Tropicos 20600124
INPN 734265
KEW urn:lsid:ipni.org:names:147-2
The Plant List kew-2610381
Open Tree Of Life 1058153
NCBI Taxonomy 341013
IUCN Red List 179300309
IPNI 147-2
iNaturalist 603440
GBIF 3830518
EOL 5517055

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Amazonia Phytotherapy Reduces Ischemia and Reperfusion Injury in the Kidneys de Oliveira BK, de Oliveira Silva E, Ventura S, Vieira GH, de Pina Victoria CD, Volpini RA, de Fátima Fernandes Vattimo M Cells 22-Jun-2023
PMCID:PMC10341095
doi:10.3390/cells12131688
PMID:37443721
Ethnobotanical inventory of medicinal plants used by Cashinahua (Huni Kuin) herbalists in Purus Province, Peruvian Amazon Horackova J, Chuspe Zans ME, Kokoska L, Sulaiman N, Clavo Peralta ZM, Bortl L, Polesny Z J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10176740
doi:10.1186/s13002-023-00586-4
PMID:37170108
Antiproliferative Activity of Krukovine by Regulating Transmembrane Protein 139 (TMEM139) in Oxaliplatin-Resistant Pancreatic Cancer Cells Lee JH, Lee SH, Lee SK, Choi JH, Lim S, Kim MS, Lee KM, Lee MW, Ku JL, Kim DH, Cho IR, Paik WH, Ryu JK, Kim YT Cancers (Basel) 07-May-2023
PMCID:PMC10177337
doi:10.3390/cancers15092642
PMID:37174108
Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021 Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T Molecules 04-Nov-2022
PMCID:PMC9656935
doi:10.3390/molecules27217579
PMID:36364404
The Impact of Oxidative Stress and AKT Pathway on Cancer Cell Functions and Its Application to Natural Products Shiau JP, Chuang YT, Tang JY, Yang KH, Chang FR, Hou MF, Yen CY, Chang HW Antioxidants (Basel) 19-Sep-2022
PMCID:PMC9495789
doi:10.3390/antiox11091845
PMID:36139919
Targeting Mutant Kirsten Rat Sarcoma Viral Oncogene Homolog in Non-Small Cell Lung Cancer: Current Difficulties, Integrative Treatments and Future Perspectives Li JX, Li RZ, Ma LR, Wang P, Xu DH, Huang J, Li LQ, Tang L, Xie Y, Leung EL, Yan PY Front Pharmacol 20-Apr-2022
PMCID:PMC9065471
doi:10.3389/fphar.2022.875330
PMID:35517800
Bioactive PI3-kinase/Akt/mTOR Inhibitors in Targeted Lung Cancer Therapy Ghareghomi S, Atabaki V, Abdollahzadeh N, Ahmadian S, Hafez Ghoran S Adv Pharm Bull 09-Oct-2021
PMCID:PMC9871280
doi:10.34172/apb.2023.003
PMID:36721812
A narrative review of the migration and invasion features of non-small cell lung cancer cells upon xenobiotic exposure: insights from in vitro studies Albuquerque C, Manguinhas R, Costa JG, Gil N, Codony-Servat J, Castro M, Miranda JP, Fernandes AS, Rosell R, Oliveira NG Transl Lung Cancer Res 01-Jun-2021
PMCID:PMC8264350
doi:10.21037/tlcr-21-121
PMID:34295671
Towards a dynamic list of Amazonian tree species ter Steege H, Mota de Oliveira S, Pitman NC, Sabatier D, Antonelli A, Guevara Andino JE, Aymard GA, Salomão RP Sci Rep 05-Mar-2019
PMCID:PMC6401171
doi:10.1038/s41598-019-40101-y
PMID:30837572
Krukovine Suppresses KRAS-Mutated Lung Cancer Cell Growth and Proliferation by Inhibiting the RAF-ERK Pathway and Inactivating AKT Pathway Lai H, Wang Y, Duan F, Li Y, Jiang Z, Luo L, Liu L, Leung EL, Yao X Front Pharmacol 22-Aug-2018
PMCID:PMC6113384
doi:10.3389/fphar.2018.00958
PMID:30186180
Astonishing diversity—the medicinal plant markets of Bogotá, Colombia Bussmann RW, Paniagua Zambrana NY, Romero C, Hart RE J Ethnobiol Ethnomed 20-Jun-2018
PMCID:PMC6011411
doi:10.1186/s13002-018-0241-8
PMID:29925407
Herbal bathing: an analysis of variation in plant use among Saramaccan and Aucan Maroons in Suriname van ‘t Klooster CI, Haabo V, Ruysschaert S, Vossen T, van Andel TR J Ethnobiol Ethnomed 15-Mar-2018
PMCID:PMC5856216
doi:10.1186/s13002-018-0216-9
PMID:29544521
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
Knowledge and use of wild edible plants in rural communities along Paraguay River, Pantanal, Brazil Bortolotto IM, Amorozo MC, Neto GG, Oldeland J, Damasceno-Junior GA J Ethnobiol Ethnomed 30-May-2015
PMCID:PMC4469002
doi:10.1186/s13002-015-0026-2
PMID:26025294
Laboratory Evaluations of the Fractions Efficacy of Annona senegalensis (Annonaceae) Leaf Extract on Immature Stage Development of Malarial and Filarial Mosquito Vectors Lame Y, Nukenine EN, Pierre DY, Elijah AE, Esimone CO J Arthropod Borne Dis 11-Mar-2015
PMCID:PMC4662794
PMID:26623434

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Proaporphines
(+)-Stepharine 193686 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
Stepharine 98455 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
> Lignans, neolignans and related compounds
6,6'-Dimethoxy-2,2'-dimethylberbaman-7,12-diol 98409 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.1055/S-1999-14017
Isofangchinoline 321937 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1055/S-1999-14017
Krukovine 10257912 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.1055/S-1999-14017
Limacine 7656034 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1055/S-1999-14017
Thalrugosine 100257 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1055/S-1999-14017
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518126 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 797.00 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44220806 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 943.10 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21607685 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 943.10 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73157287 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 943.10 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518125 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 797.00 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
Calenduloside B (8CI) 4316934 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 943.10 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
> Organoheterocyclic compounds / Isoquinolines and derivatives
14,15,16-trimethoxy-10-azatetracyclo[7.7.1.02,8.013,17]heptadeca-1,3,7,9(17),11,13,15-heptaene-5,6-dione 5379179 Click to see COC1=C2C=CNC3=C2C(=C4C3=CC(=O)C(=O)C=C4)C(=C1OC)OC 337.30 unknown https://doi.org/10.3987/COM-93-S108
Grandirubrine 630768 Click to see COC1=C(C(=C2C3=CC=C(C(=O)C=C3C4=NC=CC1=C24)O)OC)OC 337.30 unknown https://doi.org/10.3987/COM-93-S108
Isoimerubrine 9884814 Click to see COC1=CC2=C(C=CC1=O)C3=C(C(=C(C4=C3C2=NC=C4)OC)OC)OC 351.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
Pareirubrine A 197551 Click to see COC1=C(C(=C2C3=C(C(=C(C(=O)C=C3)O)OC)C4=NC=CC1=C24)OC)OC 367.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
https://doi.org/10.3987/COM-93-S108
Pareirubrine B 160367 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C4=CC(=O)C(=CC=C42)O)OC 307.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.12.007
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
1-[[4-[2-hydroxy-5-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 71773384 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC 596.70 unknown https://doi.org/10.1055/S-1999-14017
Magnoline 362563 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC 596.70 unknown https://doi.org/10.1055/S-1999-14017

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